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1.
J Neurophysiol ; 126(2): 398-412, 2021 08 01.
Article in English | MEDLINE | ID: mdl-34161139

ABSTRACT

In insects the tactile sense is important for near-range orientation and is involved in various behaviors. Nocturnal insects, such as the stick insect Carausius morosus, continuously explore their surroundings by actively moving their antennae when walking. Upon antennal contact with objects, stick insects show a targeted front-leg movement. As this reaction occurs within 40 ms, descending transfer of information from the brain to the thorax needs to be fast. So far, a number of descending interneurons have been described that may be involved in this reach-to-grasp behavior. One of these is the contralateral ON-type velocity-sensitive neuron (cONv). cONv was found to encode antennal joint-angle velocity during passive movement. Here, we characterize the transient response properties of cONv, including its dependence on joint angle range and direction. As antennal hair field afferent terminals were shown to arborize close to cONv dendrites, we test whether antennal hair fields contribute to the joint-angle velocity encoding of cONv. To do so, we conducted bilateral extracellular recordings of both cONv interneurons per animal before and after hair field ablations. Our results show that cONv responses are highly transient, with velocity-dependent differences in delay and response magnitude. As yet, the steady state activity level was maintained until the stop of antennal movement, irrespective of movement velocity. Hair field ablation caused a moderate but significant reduction of movement-induced cONv firing rate by up to 40%. We conclude that antennal proprioceptive hair fields contribute to the velocity-tuning of cONv, though further antennal mechanoreceptors must be involved, too.NEW & NOTEWORTHY Active tactile exploration and tactually induced behaviors are important for many animals. They require descending information transfer about tactile sensor movement to thoracic networks. Here, we investigate response properties and afferent input to the identified descending interneuron cONv in stick insects. cONv may be involved in tactually induced reach-to-grasp movements. We show that cONv response delay, transient and steady state are velocity-dependent and that antennal proprioceptive hair fields contribute to the velocity encoding of cONv.


Subject(s)
Arthropod Antennae/physiology , Interneurons/physiology , Sensory Receptor Cells/physiology , Animals , Arthropod Antennae/cytology , Arthropod Antennae/innervation , Ganglia, Invertebrate/cytology , Ganglia, Invertebrate/physiology , Insecta , Movement , Touch , Touch Perception
2.
Sci Rep ; 11(1): 10947, 2021 05 26.
Article in English | MEDLINE | ID: mdl-34040068

ABSTRACT

Sociality is classified as one of the major transitions in evolution, with the largest number of eusocial species found in the insect order Hymenoptera, including the Apini (honey bees) and the Bombini (bumble bees). Bumble bees and honey bees not only differ in their social organization and foraging strategies, but comparative analyses of their genomes demonstrated that bumble bees have a slightly less diverse family of olfactory receptors than honey bees, suggesting that their olfactory abilities have adapted to different social and/or ecological conditions. However, unfortunately, no precise comparison of olfactory coding has been performed so far between honey bees and bumble bees, and little is known about the rules underlying olfactory coding in the bumble bee brain. In this study, we used in vivo calcium imaging to study olfactory coding of a panel of floral odorants in the antennal lobe of the bumble bee Bombus terrestris. Our results show that odorants induce reproducible neuronal activity in the bumble bee antennal lobe. Each odorant evokes a different glomerular activity pattern revealing this molecule's chemical structure, i.e. its carbon chain length and functional group. In addition, pairwise similarity among odor representations are conserved in bumble bees and honey bees. This study thus suggests that bumble bees, like honey bees, are equipped to respond to odorants according to their chemical features.


Subject(s)
Arthropod Antennae/physiology , Bees/physiology , Brain/physiology , Olfactory Pathways/physiology , Olfactory Receptor Neurons/physiology , Smell/physiology , Animals , Appetitive Behavior/physiology , Arthropod Antennae/cytology , Arthropod Antennae/innervation , Axonal Transport , Brain/ultrastructure , Brain Mapping , Calcium/analysis , Female , Fura-2/analysis , Odorants , Social Behavior , Species Specificity
3.
J Med Entomol ; 58(1): 475-479, 2021 01 12.
Article in English | MEDLINE | ID: mdl-32740665

ABSTRACT

Research on the functions of insect chemoreceptors have primarily focused on antennae (olfactory receptors) and mouthparts (gustatory receptors). However, chemoreceptive sensilla are also present on other appendages, such as the leg tarsi and the anterior wing margin, and their specific roles in chemoreception and mosquito behavior remain largely unknown. In this study, electrophysiological analyses in an electroantennogram recording format were performed on Aedes aegypti (L., Diptera: Culicidae) antennae, mouthparts, tarsi, and wings during exposure to a variety of insect repellent and attractant compounds. The results provide evidence that the tarsi and wings can sense chemicals in a gaseous form, and that the odors produce differing responses on different appendages. The most consistent and strongest response occurred when exposed to triethylamine (TEA). Antennae and mouthparts showed nearly identical responses pattern to all tested compounds, and their rank orders of effectiveness were similar to those of fore- and mid-leg tarsi. Hindleg tarsi only responded to TEA, indicating that the hind legs are not as chemoreceptive. Wings responded to a range of odorants, but with a different rank order and voltage amplitude. Insights gleaned into the function of these appendages in insect chemoreception are discussed.


Subject(s)
Aedes/drug effects , Arthropod Antennae/physiology , Insect Repellents/administration & dosage , Pheromones/administration & dosage , Wings, Animal/physiology , Aedes/cytology , Aedes/physiology , Animals , Arthropod Antennae/cytology , Arthropod Antennae/drug effects , Chemoreceptor Cells/cytology , Chemoreceptor Cells/drug effects , Chemoreceptor Cells/physiology , Extremities/anatomy & histology , Extremities/physiology , Receptors, Odorant/physiology , Taste Perception/drug effects , Taste Perception/physiology , Wings, Animal/cytology , Wings, Animal/drug effects
4.
PLoS One ; 15(8): e0237134, 2020.
Article in English | MEDLINE | ID: mdl-32764791

ABSTRACT

Olfaction plays vital roles in the survival and reproduction of insects. The completion of olfactory recognition requires the participation of various complex protein families. However, little is known about the olfactory-related proteins in Semiothisa cinerearia Bremer et Grey, an important pest of Chinese scholar tree. In this study, we sequenced the antennal transcriptome of S. cinerearia and identified 125 olfactory-related genes, including 25 odorant-binding proteins (OBPs), 15 chemosensory proteins (CSPs), two sensory neuron membrane proteins (SNMPs), 52 odorant receptors (ORs), eight gustatory receptors (GRs) and 23 ionotropic receptors (IRs). BLASTX best hit results and phylogenetic analyses indicated that these genes were most identical to their respective orthologs from Ectropis obliqua. Further quantitative real-time PCR (qRT-PCR) analysis revealed that three ScinOBPs and three ScinORs were highly expressed in male antennae, while seven ScinOBPs and twelve ScinORs were female-specifically expressed. Our study will be useful for the elucidation of olfactory mechanisms in S. cinerearia.


Subject(s)
Arthropod Antennae/metabolism , Insect Proteins/metabolism , Moths/physiology , Smell/physiology , Animals , Arthropod Antennae/cytology , Female , Insect Proteins/genetics , Male , Membrane Proteins/genetics , Membrane Proteins/metabolism , Odorants , Olfactory Receptor Neurons/metabolism , Phylogeny , RNA-Seq , Receptors, Ionotropic Glutamate/genetics , Receptors, Ionotropic Glutamate/metabolism , Receptors, Odorant/genetics , Receptors, Odorant/metabolism
5.
Curr Biol ; 30(16): 3223-3230.e4, 2020 08 17.
Article in English | MEDLINE | ID: mdl-32559450

ABSTRACT

The insect antennal lobe (AL) contains the first synapses of the olfactory system, where olfactory sensory neurons (OSNs) contact second-order projection neurons (PNs). In Drosophila melanogaster, OSNs expressing specific receptor genes send stereotyped projections to one or two of about 50 morphologically defined glomeruli [1-3]. The mechanisms for this precise matching between OSNs and PNs have been studied extensively in D. melanogaster, where development is deterministic and independent of neural activity [4-6]. However, a number of insect lineages, most notably the ants, have receptor gene repertoires many times larger than D. melanogaster and exhibit more structurally complex antennal lobes [7-12]. Moreover, perturbation of OSN function via knockout of the odorant receptor (OR) co-receptor, Orco, results in drastic AL reductions in ants [13, 14], but not in Drosophila [15]. Here, we characterize AL development in the clonal raider ant, Ooceraea biroi. We find that, unlike in Drosophila, ORs and Orco are expressed before the onset of glomerulus formation, and Orco protein is trafficked to developing axon terminals, raising the possibility that ORs play a role during ant AL development. Additionally, ablating ant antennae at the onset of pupation results in AL defects that recapitulate the Orco mutant phenotype. Thus, early loss of functional OSN innervation reveals latent structure in the AL that develops independently of peripheral input, suggesting that the AL is initially pre-patterned and later refined in an OSN-dependent manner. This two-step process might increase developmental flexibility and thereby facilitate the rapid evolution and expansion of the ant chemosensory system.


Subject(s)
Ants/growth & development , Arthropod Antennae/cytology , Gene Expression Regulation, Developmental , Insect Proteins/metabolism , Olfactory Receptor Neurons/cytology , Receptors, Odorant/metabolism , Animals , Ants/genetics , Ants/metabolism , Arthropod Antennae/metabolism , Insect Proteins/genetics , Olfactory Receptor Neurons/metabolism , Receptors, Odorant/genetics
6.
Nat Commun ; 11(1): 1023, 2020 02 24.
Article in English | MEDLINE | ID: mdl-32094345

ABSTRACT

Connections between neuronal populations may be genetically hardwired or random. In the insect olfactory system, projection neurons of the antennal lobe connect randomly to Kenyon cells of the mushroom body. Consequently, while the odor responses of the projection neurons are stereotyped across individuals, the responses of the Kenyon cells are variable. Surprisingly, downstream of Kenyon cells, mushroom body output neurons show stereotypy in their responses. We found that the stereotypy is enabled by the convergence of inputs from many Kenyon cells onto an output neuron, and does not require learning. The stereotypy emerges in the total response of the Kenyon cell population using multiple odor-specific features of the projection neuron responses, benefits from the nonlinearity in the transfer function, depends on the convergence:randomness ratio, and is constrained by sparseness. Together, our results reveal the fundamental mechanisms and constraints with which convergence enables stereotypy in sensory responses despite random connectivity.


Subject(s)
Nerve Net/physiology , Neurons/physiology , Olfactory Pathways/physiology , Stereotyped Behavior/physiology , Animals , Arthropod Antennae/cytology , Arthropod Antennae/physiology , Behavior, Animal , Datasets as Topic , Drosophila , Grasshoppers , Mushroom Bodies/cytology , Mushroom Bodies/physiology , Odorants , Olfactory Pathways/cytology
7.
Chemosphere ; 239: 124786, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31520975

ABSTRACT

The herbicide atrazine is heavily applied in agricultural areas in the Midwestern United States and can run-off and seep into surrounding aquatic habitats where concentrations can reach over 300 ppb. It is known that acute exposures to 80 ppb atrazine cause lasting deficiencies in the chemoreception of food and mate odors. Since atrazine impairs chemosensory responses, the goal of this study was to determine the effect of atrazine on cells, including olfactory sensory neurons, located in the lateral antennules of crayfish. In this experiment, we treated crayfish for 10 days with ecologically relevant concentrations of 0, 10, 40, 80, 100 and 300 ppb (µg L-1) of atrazine. Following treatments, the distal portion of the lateral antennules was cryosectioned. We used a TdT mediated dUTP nick-end labeling (TUNEL) assay to determine if any cells had DNA damage and may be thus undergoing apoptosis. We found that as atrazine concentrations increase above 10 ppb, the number of TUNEL-positive cells, visualized in the lateral antennules, significantly increases. Our data show that atrazine exposure causes DNA damage in cells of the lateral antennules, including olfactory sensory neurons, thus leading to impairments in chemosensory abilities. Because crayfish rely heavily on chemoreception for survival, changes in their ability to perceive odors following atrazine exposure may have detrimental effects on population size.


Subject(s)
Arthropod Antennae/drug effects , Astacoidea/drug effects , Astacoidea/genetics , Atrazine/toxicity , DNA Damage/drug effects , Water Pollutants, Chemical/toxicity , Animals , Arthropod Antennae/cytology , Astacoidea/cytology , Ecotoxicology , Environmental Exposure , Female , Herbicides/toxicity , Male
8.
Proc Natl Acad Sci U S A ; 117(1): 708-716, 2020 01 07.
Article in English | MEDLINE | ID: mdl-31871198

ABSTRACT

Mosquitoes are important vectors of disease and require sources of carbohydrates for reproduction and survival. Unlike host-related behaviors of mosquitoes, comparatively less is understood about the mechanisms involved in nectar-feeding decisions, or how this sensory information is processed in the mosquito brain. Here we show that Aedes spp. mosquitoes, including Aedes aegypti, are effective pollinators of the Platanthera obtusata orchid, and demonstrate this mutualism is mediated by the orchid's scent and the balance of excitation and inhibition in the mosquito's antennal lobe (AL). The P. obtusata orchid emits an attractive, nonanal-rich scent, whereas related Platanthera species-not visited by mosquitoes-emit scents dominated by lilac aldehyde. Calcium imaging experiments in the mosquito AL revealed that nonanal and lilac aldehyde each respectively activate the LC2 and AM2 glomerulus, and remarkably, the AM2 glomerulus is also sensitive to N,N-diethyl-meta-toluamide (DEET), a mosquito repellent. Lateral inhibition between these 2 glomeruli reflects the level of attraction to the orchid scents. Whereas the enriched nonanal scent of P. obtusata activates the LC2 and suppresses AM2, the high level of lilac aldehyde in the other orchid scents inverts this pattern of glomerular activity, and behavioral attraction is lost. These results demonstrate the ecological importance of mosquitoes beyond operating as disease vectors and open the door toward understanding the neural basis of mosquito nectar-seeking behaviors.


Subject(s)
Aedes/physiology , Appetitive Behavior/physiology , Olfactory Perception/physiology , Orchidaceae/physiology , Pollination/physiology , Animals , Appetitive Behavior/drug effects , Arthropod Antennae/cytology , Arthropod Antennae/physiology , Brain/physiology , DEET/pharmacology , Female , Insect Repellents/pharmacology , Male , Mosquito Vectors/drug effects , Mosquito Vectors/physiology , Odorants , Olfactory Perception/drug effects , Olfactory Receptor Neurons/physiology , Pollination/drug effects
9.
J Invertebr Pathol ; 168: 107252, 2019 11.
Article in English | MEDLINE | ID: mdl-31585118

ABSTRACT

Varroa destructor and its associated viruses, in particular deformed wing virus (DWV), have been identified as probable causes of honey bee (Apis mellif era L.) colony losses. Evidence suggests that elevated DWV titres in bees could compromise sensory and communication abilities resulting in negative consequences for hygienic behaviour. As antennae play a central role in this behaviour, we compared antennal ultrastructure in DWV-symptomatic and asymptomatic bees. The results show that virus capsids accumulate in the basal regions of the antennal epithelium, close to the haemolymph. No virus particles were detected at the level of sensory sensilla, such as pore plates, nor within the sensory cell dendrites associated with these sensilla. However, membranous structures appeared to be more prevalent in supporting cells surrounding the dendrites of DWV-symptomatic bees. Para-crystalline arrays containing large numbers of virus particles were detected in the antennae of DWV-symptomatic bees but not in asymptomatic bees.


Subject(s)
Arthropod Antennae/virology , Bees/virology , Epithelium/virology , RNA Viruses/pathogenicity , Animals , Arthropod Antennae/cytology , Arthropod Antennae/pathology , Arthropod Antennae/ultrastructure , Electron Microscope Tomography , Epithelium/pathology , Epithelium/ultrastructure , RNA Virus Infections/diagnosis , Varroidae/virology
10.
Sci Rep ; 9(1): 10032, 2019 07 11.
Article in English | MEDLINE | ID: mdl-31296896

ABSTRACT

The greater wax moth, Galleria mellonella Linnaeus (Lepidoptera: Galleriinae), is a ubiquitous pest of the honeybee, and poses a serious threat to the global honeybee industry. G. mellonella pheromone system is unusual compared to other lepidopterans and provides a unique olfactory model for pheromone perception. To better understand the olfactory mechanisms in G. mellonella, we conducted a transcriptomic analysis on the antennae of both male and female adults of G. mellonella using high-throughput sequencing and annotated gene families potentially involved in chemoreception. We annotated 46 unigenes coding for odorant receptors, 25 for ionotropic receptors, two for sensory neuron membrane proteins, 22 for odorant binding proteins and 20 for chemosensory proteins. Expressed primarily in antennae were all the 46 odorant receptor unigenes, nine of the 14 ionotropic receptor unigenes, and two of the 22 unigenes coding for odorant binding proteins, suggesting their putative roles in olfaction. The expression of some of the identified unigenes were sex-specific, suggesting that they may have important functions in the reproductive behavior of the insect. Identification of the candidate unigenes and initial analyses on their expression profiles should facilitate functional studies in the future on chemoreception mechanisms in this species and related lepidopteran moths.


Subject(s)
Arthropod Antennae/cytology , Chemoreceptor Cells/cytology , Moths/physiology , Pheromones/genetics , Receptors, Odorant/genetics , Animals , Arthropod Antennae/metabolism , Chemoreceptor Cells/metabolism , Female , Gene Expression Profiling , Male , Moths/genetics , Pheromones/metabolism , Transcriptome/genetics
11.
PLoS One ; 14(5): e0216294, 2019.
Article in English | MEDLINE | ID: mdl-31048879

ABSTRACT

Barnacle settlement involves sensing of a variety of exogenous cues. A pair of antennules is the main sensory organ that the cyprid larva uses to explore the surface. Antennules are equipped with a number of setae that have both chemo- and mechanosensing function. The current study explores the repertoire of sensory receptors in Balanus improvisus cyprid antennules with the goal to better understand sensory systems involved in the settling behavior of this species. We carried out transcriptome sequencing of dissected B. improvisus cyprid antennules. The generated transcriptome assembly was used to search for sensory receptors using HMM models. Among potential chemosensory genes, we identified the ionotropic receptors IR25a, IR8a and IR93a, and several divergent IR candidates to be expressed in the cyprid antennules. We found one gustatory-like receptor but no odorant receptors, chemosensory or odorant-binding proteins. Apart from chemosensory receptors, we also identified 13 potential mechanosensory genes represented by several transient receptor potential channels (TRP) subfamilies. Furthermore, we analyzed changes in expression profiles of IRs and TRPs during the B. improvisus settling process. Several of the sensory genes were differentially expressed during the course of larval settlement. This study gives expanded knowledge about the sensory systems present in barnacles, a taxonomic group for which only limited information about receptors is currently available. It furthermore serves as a starting point for more in depth studies of how sensory signaling affects settling behavior in barnacles with implications for preventing biofouling.


Subject(s)
Arthropod Antennae/metabolism , Arthropod Proteins , Chemoreceptor Cells , Ligand-Gated Ion Channels , Thoracica , Animals , Arthropod Antennae/cytology , Arthropod Proteins/genetics , Arthropod Proteins/metabolism , Chemoreceptor Cells/cytology , Chemoreceptor Cells/metabolism , Ligand-Gated Ion Channels/genetics , Ligand-Gated Ion Channels/metabolism , Thoracica/anatomy & histology , Thoracica/genetics , Thoracica/metabolism
12.
Elife ; 72018 12 21.
Article in English | MEDLINE | ID: mdl-30576281

ABSTRACT

Habituation is the process that enables salience filtering, precipitating perceptual changes that alter the value of environmental stimuli. To discern the neuronal circuits underlying habituation to brief inconsequential stimuli, we developed a novel olfactory habituation paradigm, identifying two distinct phases of the response that engage distinct neuronal circuits. Responsiveness to the continuous odor stimulus is maintained initially, a phase we term habituation latency and requires Rutabaga Adenylyl-Cyclase-depended neurotransmission from GABAergic Antennal Lobe Interneurons and activation of excitatory Projection Neurons (PNs) and the Mushroom Bodies. In contrast, habituation depends on the inhibitory PNs of the middle Antenno-Cerebral Track, requires inner Antenno-Cerebral Track PN activation and defines a temporally distinct phase. Collectively, our data support the involvement of Lateral Horn excitatory and inhibitory stimulation in habituation. These results provide essential cellular substrates for future analyses of the molecular mechanisms that govern the duration and transition between these distinct temporal habituation phases. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter).


Subject(s)
Arthropod Antennae/physiology , Drosophila melanogaster/drug effects , Interneurons/physiology , Mushroom Bodies/physiology , Olfactory Pathways/physiology , Olfactory Receptor Neurons/physiology , Smell/physiology , Acetates/pharmacology , Adenylyl Cyclases/genetics , Adenylyl Cyclases/metabolism , Animals , Arthropod Antennae/cytology , Arthropod Antennae/drug effects , Benzaldehydes/pharmacology , Diacetyl/pharmacology , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Drosophila melanogaster/cytology , Drosophila melanogaster/physiology , Gene Expression , Hydroxyurea/toxicity , Interneurons/cytology , Interneurons/drug effects , Mushroom Bodies/cytology , Mushroom Bodies/drug effects , Octanols/pharmacology , Odorants/analysis , Olfactory Pathways/cytology , Olfactory Pathways/drug effects , Olfactory Receptor Neurons/cytology , Olfactory Receptor Neurons/drug effects , Synaptic Transmission/physiology
13.
Yale J Biol Med ; 91(4): 457-469, 2018 12.
Article in English | MEDLINE | ID: mdl-30588211

ABSTRACT

Chemical communication involves the production, transmission, and perception of odors. Most adult insects rely on chemical signals and cues to locate food resources, oviposition sites or reproductive partners and, consequently, numerous odors provide a vital source of information. Insects detect these odors with receptors mostly located on the antennae, and the diverse shapes and sizes of these antennae (and sensilla) are both astonishing and puzzling: what selective pressures are responsible for these different solutions to the same problem - to perceive signals and cues? This review describes the selection pressures derived from chemical communication that are responsible for shaping the diversity of insect antennal morphology. In particular, we highlight new technologies and techniques that offer exciting opportunities for addressing this surprisingly neglected and yet crucial component of chemical communication.


Subject(s)
Arthropod Antennae/cytology , Arthropod Antennae/physiology , Biological Evolution , Odorants , Animals
14.
Insect Biochem Mol Biol ; 101: 32-46, 2018 10.
Article in English | MEDLINE | ID: mdl-30026095

ABSTRACT

The Oriental fruit fly, Bactrocera dorsalis, is a highly destructive pest of various fruits. The reproductive and host-finding behaviors of this species are affected by several plant semiochemicals that are perceived through chemosensory receptors. However, the chemosensory mechanisms by which this perception occurs have not been fully elucidated. We conducted RNA sequencing analysis of the chemosensory organs of B. dorsalis to identify the genes coding for chemosensory receptors. We identified 60 olfactory receptors (ORs), 17 gustatory receptors and 23 ionotropic receptors-including their homologs and variants-from the transcriptome of male antennae and proboscises. We functionally analyzed ten ORs co-expressed with the obligatory co-receptor ORCO in Xenopus oocytes to identify their ligands. We tested 24 compounds including attractants for several Bactrocera species and volatiles from the host fruits of B. dorsalis. We found that BdorOR13a co-expressed with ORCO responded robustly to 1-octen-3-ol. BdorOR82a co-expressed with ORCO responded significantly to geranyl acetate, but responded weakly to farnesenes (a mixture of isomers) and linalyl acetate. These four compounds were subsequently subjected to behavioral bioassays. When each of the aforementioned compound was presented in combination with a sphere model as a visual cue to adult flies, 1-octen-3-ol, geranyl acetate, and farnesenes significantly enhanced landing behavior in mated females, but not in unmated females or males. These results suggest that the ORs characterized in the present study are involved in the perception of plant volatiles that affect host-finding behavior in B. dorsalis.


Subject(s)
Insect Proteins/genetics , Octanols/pharmacology , Olfactory Receptor Neurons/physiology , Receptors, Odorant/genetics , Tephritidae/physiology , Transcriptome , Acetates/chemistry , Acetates/pharmacology , Acyclic Monoterpenes , Animals , Arthropod Antennae/cytology , Arthropod Antennae/drug effects , Arthropod Antennae/physiology , Biological Assay , Female , Gene Expression Regulation , Insect Proteins/metabolism , Male , Monoterpenes/chemistry , Monoterpenes/pharmacology , Octanols/chemistry , Olfactory Receptor Neurons/cytology , Olfactory Receptor Neurons/drug effects , Oocytes/cytology , Oocytes/drug effects , Oocytes/metabolism , Patch-Clamp Techniques , Pheromones/chemistry , Pheromones/pharmacology , Phylogeny , Receptors, Odorant/classification , Receptors, Odorant/metabolism , Tephritidae/classification , Tephritidae/cytology , Tephritidae/drug effects , Terpenes/chemistry , Terpenes/pharmacology , Xenopus laevis
15.
Nat Commun ; 9(1): 2232, 2018 06 08.
Article in English | MEDLINE | ID: mdl-29884811

ABSTRACT

Drosophila olfactory local interneurons (LNs) in the antennal lobe are highly diverse and variable. How and when distinct types of LNs emerge, differentiate, and integrate into the olfactory circuit is unknown. Through systematic developmental analyses, we found that LNs are recruited to the adult olfactory circuit in three groups. Group 1 LNs are residual larval LNs. Group 2 are adult-specific LNs that emerge before cognate sensory and projection neurons establish synaptic specificity, and Group 3 LNs emerge after synaptic specificity is established. Group 1 larval LNs are selectively reintegrated into the adult circuit through pruning and re-extension of processes to distinct regions of the antennal lobe, while others die during metamorphosis. Precise temporal control of this pruning and cell death shapes the global organization of the adult antennal lobe. Our findings provide a road map to understand how LNs develop and contribute to constructing the olfactory circuit.


Subject(s)
Drosophila melanogaster/metabolism , Interneurons/metabolism , Olfactory Pathways/metabolism , Olfactory Receptor Neurons/metabolism , Animals , Animals, Genetically Modified , Arthropod Antennae/cytology , Arthropod Antennae/growth & development , Arthropod Antennae/metabolism , Drosophila melanogaster/genetics , Drosophila melanogaster/growth & development , Interneurons/classification , Larva/growth & development , Larva/metabolism , Microscopy, Confocal , Models, Neurological , Morphogenesis , Nerve Net/cytology , Nerve Net/growth & development , Nerve Net/metabolism , Olfactory Pathways/cytology , Olfactory Pathways/growth & development , Olfactory Receptor Neurons/classification , Synaptic Transmission , Time Factors
16.
Insect Biochem Mol Biol ; 97: 31-39, 2018 06.
Article in English | MEDLINE | ID: mdl-29698698

ABSTRACT

Plant volatiles are vital cues in the location of hosts for feeding and oviposition for Lepidoptera moths. The noctuid Helicoverpa assulta is a typical polyphagous moth, regarded as a good model for studying the olfactory reception of plant volatiles. In this study, four full-length genes encoding odorant receptors HassOR24, HassOR40, HassOR41, and HassOR55 expressed in antenna in H. assulta were functionally characterized. The highly expressed HassOR40 was narrowly tuned to a few structurally-related plant volatiles: geranyl acetate, geraniol and nerolidol. By systematically analyzing responses of single neuron in both trichoid sensilla and basiconic sensilla using single sensillum recording, the specific neuron B in one type of short trichoid sensilla was found to be mainly activated by the same chemicals as HassOR40 with high sensitivity, and with no significant difference between male and female neurons. Thus, a clear "receptor-neuron" relationship in H. assulta was demonstrated here, suggesting that HassOR40/HassOrco are expressed in neuron B of short trichoid sensilla. The active tobacco volatile nerolidol, recognized by this receptor-neuron line, elicits significant behavioral attraction of both sexes in H. assulta adults. The results indicate that we identified a receptor-neuron route for the peripheral coding of a behaviorally relevant host volatile in H. assulta.


Subject(s)
Arthropod Antennae/metabolism , Insect Proteins/biosynthesis , Lepidoptera/metabolism , Neurons/metabolism , Receptors, Odorant/biosynthesis , Volatile Organic Compounds/metabolism , Animals , Arthropod Antennae/cytology , Arthropod Antennae/innervation , Gene Expression Regulation/physiology , Insect Proteins/genetics , Lepidoptera/cytology , Lepidoptera/genetics , Neurons/cytology , Receptors, Odorant/genetics
17.
Sci Rep ; 8(1): 4950, 2018 03 21.
Article in English | MEDLINE | ID: mdl-29563503

ABSTRACT

The imaginal discs of the genetically tractable model organism Drosophila melanogaster have been used to study cell-fate specification and plasticity, including homeotic changes and regeneration-induced transdetermination. The identity of the reprogramming mechanisms that induce plasticity has been of great interest in the field. Here we identify a change from antennal fate to eye fate induced by a Distal-less-GAL4 (DllGAL4) P-element insertion that is a mutant allele of Dll and expresses GAL4 in the antennal imaginal disc. While this fate change is not induced by tissue damage, it appears to be a hybrid of transdetermination and homeosis as the GAL4 expression causes upregulation of Wingless, and the Dll mutation is required for the fate change. Neither GAL4 expression nor a Dll mutation on its own is able to induce antenna-to-eye fate changes. This plasticity appears to be unique to the DllGAL4 line, possibly due to cellular stress induced by the high GAL4 expression combined with the severity of the Dll mutation. Thus, we propose that even in the absence of tissue damage, other forms of cellular stress caused by high GAL4 expression can induce determined cell fates to change, and selector gene mutations can sensitize the tissue to these transformations.


Subject(s)
Arthropod Antennae/growth & development , Drosophila melanogaster/growth & development , Gene Expression Regulation, Developmental , Homeodomain Proteins/physiology , Imaginal Discs/growth & development , Transcription Factors/physiology , Animals , Animals, Genetically Modified/genetics , Animals, Genetically Modified/growth & development , Arthropod Antennae/cytology , Cell Plasticity/genetics , DNA-Binding Proteins/genetics , Drosophila Proteins/metabolism , Drosophila melanogaster/genetics , Enhancer Elements, Genetic/genetics , Female , Imaginal Discs/cytology , Male , Mutation , Saccharomyces cerevisiae Proteins/genetics , Transcription Factors/genetics , Transgenes/genetics , Up-Regulation , Wnt1 Protein/metabolism
18.
PLoS One ; 13(1): e0191425, 2018.
Article in English | MEDLINE | ID: mdl-29351552

ABSTRACT

The honeybee olfactory pathway comprises an intriguing pattern of convergence and divergence: ~60.000 olfactory sensory neurons (OSN) convey olfactory information on ~900 projection neurons (PN) in the antennal lobe (AL). To transmit this information reliably, PNs employ relatively high spiking frequencies with complex patterns. PNs project via a dual olfactory pathway to the mushroom bodies (MB). This pathway comprises the medial (m-ALT) and the lateral antennal lobe tract (l-ALT). PNs from both tracts transmit information from a wide range of similar odors, but with distinct differences in coding properties. In the MBs, PNs form synapses with many Kenyon cells (KC) that encode odors in a spatially and temporally sparse way. The transformation from complex information coding to sparse coding is a well-known phenomenon in insect olfactory coding. Intrinsic neuronal properties as well as GABAergic inhibition are thought to contribute to this change in odor representation. In the present study, we identified intrinsic neuronal properties promoting coding differences between PNs and KCs using in-situ patch-clamp recordings in the intact brain. We found very prominent K+ currents in KCs clearly differing from the PN currents. This suggests that odor coding differences between PNs and KCs may be caused by differences in their specific ion channel properties. Comparison of ionic currents of m- and l-ALT PNs did not reveal any differences at a qualitative level.


Subject(s)
Bees/cytology , Bees/physiology , Olfactory Pathways/cytology , Olfactory Pathways/physiology , Action Potentials , Animals , Arthropod Antennae/cytology , Arthropod Antennae/physiology , Brain/cytology , Brain/physiology , Electrophysiological Phenomena , Ion Channels/physiology , Ion Transport , Mushroom Bodies/cytology , Mushroom Bodies/physiology , Olfactory Receptor Neurons/cytology , Olfactory Receptor Neurons/physiology , Patch-Clamp Techniques , Smell/physiology
19.
PLoS Comput Biol ; 13(12): e1005870, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29194457

ABSTRACT

Long-distance olfactory search behaviors depend on odor detection dynamics. Due to turbulence, olfactory signals travel as bursts of variable concentration and spacing and are characterized by long-tail distributions of odor/no-odor events, challenging the computing capacities of olfactory systems. How animals encode complex olfactory scenes to track the plume far from the source remains unclear. Here we focus on the coding of the plume temporal dynamics in moths. We compare responses of olfactory receptor neurons (ORNs) and antennal lobe projection neurons (PNs) to sequences of pheromone stimuli either with white-noise patterns or with realistic turbulent temporal structures simulating a large range of distances (8 to 64 m) from the odor source. For the first time, we analyze what information is extracted by the olfactory system at large distances from the source. Neuronal responses are analyzed using linear-nonlinear models fitted with white-noise stimuli and used for predicting responses to turbulent stimuli. We found that neuronal firing rate is less correlated with the dynamic odor time course when distance to the source increases because of improper coding during long odor and no-odor events that characterize large distances. Rapid adaptation during long puffs does not preclude however the detection of puff transitions in PNs. Individual PNs but not individual ORNs encode the onset and offset of odor puffs for any temporal structure of stimuli. A higher spontaneous firing rate coupled to an inhibition phase at the end of PN responses contributes to this coding property. This allows PNs to decode the temporal structure of the odor plume at any distance to the source, an essential piece of information moths can use in their tracking behavior.


Subject(s)
Appetitive Behavior/physiology , Arthropod Antennae/physiology , Olfactory Pathways/physiology , Olfactory Receptor Neurons/physiology , Pheromones/metabolism , Animals , Arthropod Antennae/cytology , Computational Biology/methods , Male , Moths/physiology , Olfactory Receptor Neurons/metabolism
20.
Sci Rep ; 7(1): 15470, 2017 11 13.
Article in English | MEDLINE | ID: mdl-29133804

ABSTRACT

Olfaction in insects is essential for host identification, mating and oviposition, in which olfactory proteins are responsible for chemical signaling. Here, we determined the transcriptomes of male and female adult antennae of Anoplophora chinensis, the citrus longhorned beetle. Among 59,357 unigenes in the antennal assembly, we identified 46 odorant-binding proteins, 16 chemosensory proteins (CSPs), 44 odorant receptors, 19 gustatory receptors, 23 ionotropic receptors, and 3 sensory neuron membrane proteins. Among CSPs, AchiCSP10 was predominantly expressed in antennae (compared with legs or maxillary palps), at a significantly higher level in males than in females, suggesting that AchiCSP10 has a role in reception of female sex pheromones. Many highly expressed genes encoding CSPs are orthologue genes of A. chinensis and Anoplophora glabripennis. Notably, AchiPBP1 and AchiPBP2 showed 100% and 96% identity with AglaPBP1 and AglaPBP2 from A. glabripennis, with similar expression profiles in the two species; PBP2 was highly expressed in male antennae, whereas PBP1 was expressed in all three tissues in both males and females. These results provide a basis for further studies on the molecular chemoreception mechanisms of A. chinensis, and suggest novel targets for control of A. chinensis.


Subject(s)
Arthropod Antennae/metabolism , Coleoptera/genetics , Insect Proteins/genetics , Smell/genetics , Transcriptome/genetics , Animals , Arthropod Antennae/cytology , Female , Gene Expression Profiling , Genes, Insect/genetics , Male , Olfactory Receptor Neurons/metabolism , Receptors, Odorant
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